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hereditary desmoid disease (DOID:0111349)
Alliance: disease page
Synonyms: familial infiltrative fibromatosis; FIF
Alt IDs: OMIM:135290, MESH:C535944, UMLS_CUI:C1851124
Definition: A syndrome characterized by extraintestinal manifestation of familial adenomatous polyposis that has_material_basis_in in some cases by extreme 3' mutation in APC on 5q22.2.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory